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HJV mutations causing hemochromatosis: variable phenotypic expression in a pair of twins.
Vadivelan, Akhila; Zhang, Sarah; Srole, Daniel N; Marcus, Elizabeth A; Neto, George Carvalho; Nemeth, Elizabeta; Ganz, Tomas; De Oliveira, Satiro.
Afiliación
  • Vadivelan A; Division of Pediatrics, Division of Hematology/Oncology, UCLA, Los Angeles; Center for Iron Disorders, Department of Medicine, UCLA. av.akhila@gmail.com.
  • Zhang S; Division of Pathology, UCLA.
  • Srole DN; Center for Iron Disorders, Department of Medicine, UCLA.
  • Marcus EA; Division of Pediatric, Pediatric Gastroenterology, Hepatology, and Nutrition, UCLA.
  • Neto GC; Corporate Authorship-Undiagnosed Diseases Network, Institute for Precision Health.
  • Nemeth E; Center for Iron Disorders, Department of Medicine, UCLA.
  • Ganz T; Center for Iron Disorders, Department of Medicine, UCLA, Los Angeles; Division of Medicine and Pathology, UCLA.
  • De Oliveira S; Division of Pediatrics, Division of Hematology/Oncology, UCLA.
Haematologica ; 109(8): 2741-2744, 2024 08 01.
Article en En | MEDLINE | ID: mdl-38450514
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Proteína de la Hemocromatosis / Hemocromatosis / Mutación Límite: Child / Female / Humans / Infant / Newborn Idioma: En Revista: Haematologica Año: 2024 Tipo del documento: Article
Texto completo
Añadir a Mi BVS
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Proteína de la Hemocromatosis / Hemocromatosis / Mutación Límite: Child / Female / Humans / Infant / Newborn Idioma: En Revista: Haematologica Año: 2024 Tipo del documento: Article